FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ADVIA CENTAUR RUBELLA IGG ASSAY
K Number: K003412
·
Decision Apr 13, 2001
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
96
Review Days
162
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Basic Information
- Device Name
- ADVIA CENTAUR RUBELLA IGG ASSAY
- K Number
- K003412
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3510
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bayer Corp.
- Date Received
- November 2, 2000
- Decision Date
- April 13, 2001
- Product Code
- LFX
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LFX | Enzyme Linked Immunoabsorbent Assay, Rubella | FDA class 2 | Microbiology |
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